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On page 244 showing 4861 ~ 4880 out of 256,031 results
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  • RRID:CVCL_4N12

https://web.expasy.org/cellosaurus/CVCL_4N12

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01386, RRID:CVCL_4N12 Copy   


  • RRID:CVCL_7319

https://web.expasy.org/cellosaurus/CVCL_7319

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_7319 Copy   


  • RRID:CVCL_AV86

https://web.expasy.org/cellosaurus/CVCL_AV86

Organism: Homo sapiens (Human)
Disease: Hereditary orotic aciduria
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01406, RRID:CVCL_AV86 Copy   


  • RRID:CVCL_0M09

https://web.expasy.org/cellosaurus/CVCL_0M09

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: Coriell Cat# GM01442, RRID:CVCL_0M09 Copy   


  • RRID:CVCL_JB82

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_JB82

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_JB82 Copy   


  • RRID:CVCL_X246

https://web.expasy.org/cellosaurus/CVCL_X246

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.

Proper citation: RRID:CVCL_X246 Copy   


  • RRID:CVCL_7318

https://web.expasy.org/cellosaurus/CVCL_7318

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Puerto Rican.

Proper citation: Coriell Cat# GM01380, RRID:CVCL_7318 Copy   


  • RRID:CVCL_4N08

https://web.expasy.org/cellosaurus/CVCL_4N08

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01354, RRID:CVCL_4N08 Copy   


  • RRID:CVCL_X248

https://web.expasy.org/cellosaurus/CVCL_X248

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01441, RRID:CVCL_X248 Copy   


  • RRID:CVCL_1Y26

https://web.expasy.org/cellosaurus/CVCL_1Y26

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_1Y26 Copy   


  • RRID:CVCL_DD67

https://web.expasy.org/cellosaurus/CVCL_DD67

Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01436, RRID:CVCL_DD67 Copy   


  • RRID:CVCL_1V14

https://web.expasy.org/cellosaurus/CVCL_1V14

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_1V14 Copy   


  • RRID:CVCL_4N13

https://web.expasy.org/cellosaurus/CVCL_4N13

Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_4N13 Copy   


  • RRID:CVCL_0P92

https://web.expasy.org/cellosaurus/CVCL_0P92

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;21)(q11;p11) (PubMed=10377420)., Population: African American.

Proper citation: RRID:CVCL_0P92 Copy   


  • RRID:CVCL_4N10

https://web.expasy.org/cellosaurus/CVCL_4N10

Organism: Homo sapiens (Human)
Disease: Cutis laxa
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM01377, RRID:CVCL_4N10 Copy   


  • RRID:CVCL_F657

https://web.expasy.org/cellosaurus/CVCL_F657

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM01416, RRID:CVCL_F657 Copy   


  • RRID:CVCL_AV86

https://web.expasy.org/cellosaurus/CVCL_AV86

Organism: Homo sapiens (Human)
Disease: Hereditary orotic aciduria
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_AV86 Copy   


  • RRID:CVCL_J115

https://web.expasy.org/cellosaurus/CVCL_J115

Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: RRID:CVCL_J115 Copy   


  • RRID:CVCL_D872

https://web.expasy.org/cellosaurus/CVCL_D872

Organism: Homo sapiens (Human)
Disease: Maple syrup urine disease
Category: Transformed cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_D872 Copy   


  • RRID:CVCL_0M10

https://web.expasy.org/cellosaurus/CVCL_0M10

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.

Proper citation: RRID:CVCL_0M10 Copy   



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